Expression and secretion of heterologous polypeptides from caulobacter

ABSTRACT

DNA constructs are provided which code for at least the extreme C-terminal amino acids of the  rsa A protein of  Caulobacter crescentus  fused with heterologous polypeptides. Baterial cells containing, or which express the DNA constructs and secrete the resulting protein are also provided. Chimeric proteins including the C-terminal amino acids of the  rsa A protein are provided, including chimeric proteins comprising antigenic epitopes of the Infectious Hematopoietic Necrosis Virus.

RELATED APPLICATIONS

[0001] This application is a continuation-in-part of application Ser. No. 08/194,290 filed Feb. 9, 1994, which is a continuation-in-part of application Ser. No. 07/895,367 filed Jun. 9, 1992 now abandoned.

FIELD OF INVENTION

[0002] This invention relates to the expression and secretion of heterologous peptides, from Caulobacter wherein the heterologous polypeptide is fused with the surface layer protein (S-layer protein) of the bacterium, or a portion of the S-layer protein.

BACKGROUND OF THE INVENTION

[0003] Bacterial surface proteins have been used as carriers for foreign (heterologous) polypeptides (particularly in Salmonella and E. coli) for various purposes, including the development of live vaccines. In some instances, the heterologous material is expressed as a fusion product with a surface protein of the bacterium. Generally, the use of such surface proteins as a vehicle for expression and/or presentation of heterologous polypeptides has been limited by the characteristics of a particular surface protein. The lipopolysaccharide layer of a bacterium, which tends to stimulate a strong immune response, covers the integral outer membrane proteins of the organism and potentially affects efficient presentation of a cloned epitope. Where the surface protein is functional (for example, as part of a filamentous portion of a bacterial cell surface) there will be limited opportunities to express a fusion product and still retain the surface protein's function. Generally, the organisms that have been used for these purposes have been chosen because of the advantages presented in respect of the organism's relationship to its host.

[0004] Many genera of bacteria assemble layers composed of repetitive, regularly aligned, proteinaceous sub-units on the outer surface of the cell. These layers are essentially two-dimensional paracrystalline arrays, and being the outer molecular layer of the organism, directly interface with the environment. Such layers are commonly known as S-layers and are found on members of every taxonomic group of walled bacteria including: Archaebacteria; Chlamydia; Cyanobacteria; Acinetobacter; Bacillus; Aquaspirrillum; Caulobacter; Clostridium; Chromatium. Typically, an S-layer will be composed of an intricate, geometric array of at least one major protein having a repetitive regular structure. In many cases, such as in Caulobacter, the S-layer protein is synthesized by the cell in large quantities and the S-layer completely envelopes the cell and thus appears to be a protective layer.

[0005] Caulobacter are natural inhabitants of most soil and freshwater environments and may persist in waste water treatment systems and effluents. The bacteria alternate between a stalked cell that is attached to a surface, and an adhesive motile dispersal cell that searches to find a new surface upon which to stick and convert to a stalked cell. The bacteria attach tenaciously to nearly all surfaces and do so without producing the extracelluar enzymes or polysaccharide “slimes” that are characteristic of most other surface attached bacteria. They have simple requirements for growth. The organism is ubiquitous in the environment and has been isolated from oligotrophic to mesotrophic situations. Caulobacters are known for their ability to tolerate low nutrient level stresses, for example, low phosphate levels. This nutrient can be limiting in many leachate waste streams, especially those with high levels of iron or calcium.

[0006] The S-layer of Caulobacter crescentus has been well characterised. Nearly all freshwater isolates of Caulobacter elaborate an S-layer visibly indistinguishable from the S-layer produced by Caulobacter crescentus strains CB2 and CB15. The S-layer proteins from these strains have approximately 100,000 m.w. The protein has been characterized both structurally and chemically. It is composed of ring-like structures spaced at 22 nm intervals arranged in a hexagonal manner on the outer membrane. The S-layer is bound to the bacterial surface and may be removed by low pH treatment or by treatment with a calcium chelator such as EDTA.

[0007] The S-layer proteins of different strains of Caulobacter have significant similarity. Thus a cloned S-layer protein gene of one Caulobacter strain is useful to retrieve the corresponding genes in other Caulobacter strains (see: Walker, S. G., et al. 1992). Isolation and Comparison of the Paracrystalline Surface Layer Proteins of Freshwater Caulobacters. J. Bacteriol. 174: 1783-1792; and, MacRae, J. O. and, J. Smit. 1991. “Characterization of Caulobacters Isolated from Wastewater Treatment Systems. Applied and Environmental Microbiology 57:751-758).

[0008] Expression, secretion and optionally, presentation, of a heterologous polypeptide as a fusion product with the S-layer protein of Caulobacter provides advantages not previously seen in systems using organisms such as E. coli and Salmonella where fusion products of other kinds of surface proteins have been expressed. All known Caulobacter strains are believed to be harmless and are nearly ubiquitous in aquatic environments. In contrast, many Salmonella and E. coli strains are pathogens. Consequently, expression and secretion of a heterologous polypeptide using Caulobacter as a vehicle will have the advantage that the expression system will be stable in a variety of outdoor environments and may not present problems associated with the use of a pathogenic organism. Furthermore, Caulobacter are natural biofilm forming species and may be adapted for use in fixed biofilm bioreactors. The quantity of S-layer protein that is synthesized and is secreted by Caulobacter is high, reaching 12% of the cell protein. The unique characteristics of the repetitive, two-dimensional S-layer would also make such bacteria ideal for use as an expression system, or as a presentation surface for heterologous polypeptides. This is desirable in a live vaccine to maximize presentation of the antigen or antigenic epitope. In addition, use of such a presentation surface to achieve maximal exposure of a desired polypeptide to the environment results in such bacteria being particularly suited for use in bioreactors or as carriers for the polypeptide in aqueous or terrestrial outdoor environments.

SUMMARY OF INVENTION

[0009] This invention provides a method of expressing and presenting to the environment of a Caulobacter, a polypeptide that is heterologous to an S-layer protein of the Caulobacter, which comprises cloning a coding sequence for the polypeptide in-frame into a S-layer protein gene of Caulobacter, or a portion of said S-layer protein gene, whereby the polypeptide is expressed and secreted by the Caulobacter as a chimeric protein comprising the heterologous protein and all or part of the S-layer protein.

[0010] This invention provides a DNA construct for the aforemention chimeric protein, and a bacterium comprising such a DNA construct, wherein the DNA construct encodes all or part of a S-layer protein, and one or more in-frame sequences encoding one or more heterologous proteins.

[0011] This invention provides a DNA construct comprising in sequence, one or more restriction sites for facilitating insertion of DNA to the construct and, DNA encoding at least the C-terminal region of the rsaA protein of C. crescentus, wherein the C-terminal region comprises at least amino acids 944-1026 of the rsaA protein.

[0012] This invention provides the DNA construct comprising DNA encoding a heterologous polypeptide sequence not present in the rsaA protein upstream from and in-frame with DNA encoding at least the C-terminal region of the rsaA protein of C. crescentus, wherein the C-terminal regional comprises at least amino acids 944-1026 of the rsaA protein.

[0013] This invention also provides a secreted protein obtained from the cell surface or cell medium of a Caulobacter cell expressing the aforementioned DNA construct wherein protein comprises the heterologous polypeptide and the C-terminal region of the protein is at least amino acids 944-1026 of rsaA protein.

DESCRIPTION OF THE DRAWINGS

[0014] For better understanding of this invention, reference may be made to the preferred embodiments and examples described below, and the accompanying drawings in which:

[0015]FIG. 1 is the sequence of a Carrier cassette which may be cloned into the PstI/BamHI site of pUC9 to deliver a gene sequence of interest to sites within a Caulobacter crescentus S-layer protein rsaA gene (SEQ ID NO:1).

[0016]FIG. 2 is a restriction map of a plasmid based promoter-less version of the rsaA gene (pTZ18U:rsaAΔP) containing restriction sites and which may be used to accept heterologous DNA of interest.

[0017]FIG. 3 is the nucleotide sequence of linker BamHI-7165K (SEQ ID NO:2; and SEQ ID NO:3) carried in plasmid pUC9B (pUC7165K), which may be used for mutagenesis at sites created in rsaA by a specific or non-specific endonuclease.

[0018]FIG. 4 is the nucleotide sequence a linker BamHI-6571K (SEQ ID NO:4; and SEQ ID NO:5) carried in plasmid pTZ19 (pTZ6571K) which may be used for mutagenesis at sites created in rsaA by a specific or non-specific endonuclease.

[0019]FIG. 5 is a map of insertion events at TaqI sites in the rsaA gene identified by amino acid number of the insertion site in the S-layer protein and scored according to whether the S-layer is produced in the modified organism.

[0020]FIG. 6 (comprising FIGS. 6a, b, and c) shows the complete nucleotide sequence of the C. crescentus rsaA gene (SEQ ID NO:6) and the predicted translational product in the single letter amino acid code. The −35 and −10 sites of the promoter region as well as the start of transcription and the Shine-Dalgarno sequence are indicated. Partial amino acid sequences determined by Edman degradation of rsaA protein and of sequenced peptides obtained after cleavage with V8 protease are indicated by contiguous underlining. The putative transcription terminator palindrome is indicated with arrowed lines. The region encoding the glycine-aspartate repeats is indicated by underlined amino acid code letters. This region includes five aspartic acids that may be involved in the binding of calcium ions. The GenBank accession number is M84760.

[0021]FIG. 7 is a bar graph showing the approximate location by amino acid block of 54 permissive sites in the rsaA gene corresponding to TaqI, HinPI, AciI, and MspI sites described in Example 3.

[0022]FIG. 8 is a portion of an amino acid sequence (SEQ ID NO: 8) from P. aeruginosa PAK pilin in which the 12 amino acid pilus peptide epitope referred to in Example 5 is identified by superscript numerals 1-12.

[0023]FIG. 9 is the nucleotide coding sequence and corresponding amino acid sequence (SEQ ID NO:9) in respect of the 184 amino acid sequence corresponding to amino acids 270-453 of the IHNV surface glycoprotein described in Example 6.

[0024]FIG. 10 is the amino acid sequence of the synthetic cadmium binding peptide referred to in Example 4. The cadmium binding site is shown in the figure.

[0025]FIG. 11 shows locations of some of the sites in rsaA in which single and multiple copies of the pilus peptide described in Example 5 was expressed and secreted as part of a chimeric rsaA protein.

[0026]FIG. 12 shows a portion of pUC8 containing various C-terminal fragments of rsaA as described in Example 7.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0027] A preferred organism for use in this invention is Caulobacter, particularly C. crescentus. Most preferred are C. crescentus strains CB2 and CB15 and variants of those strains such as CB15A which contain homologs of the rsaA gene encoding the 1026 amino acid paracrystalline S-layer protein described in: Gilchrist, A. et al. 1992. “Nucleotide Sequence Analysis Of The Gene Encoding the Caulobacter crescentus Paracrystalline Surface Layer Protein”. Can. J. Microbiol. 38:193-208.

[0028] It may also be desirable to use Caulobacter strains which either are incapable of themselves in expressing or secreting S-layer protein or which shed the S-layer protein upon secretion and do not form an intact S-layer. Examples of the former category are the variants CB2A and CB15AKSac described in Smit, J., and N. Agabian. 1984. “Cloning of the Major Protein of the Caulobacter crescentus Periodic Surface Layer: Detection and Other Characterization of the Cloned Peptide by Protein Expression Assays”. J. Bacteriol. 160:1137-1145.; and, Edwards, P., and J. Smit. 1991. “A Transducing Bacteriophage for Caulobacter crescentus Uses the Paracrystalline Surface Layer Protein as Receptor”. J. Bacteriol. 173, 5568-5572. Examples of shedding strains are CB15Ca5 and CB15Ca10 described in Edwards and Smit (1991) [supra], and the smooth lipopolysaccharide deficient mutants described in Walker, S. G. et al. 1994. “Characterization of Mutants of Caulobacter crescentus Defective in Surface Attachment of the Paracrystalline Surface Layer”. J. Bacteriol. 176:6312-6323.

[0029] A heterologous polypeptide referred to herein may be any peptide, polypeptide, protein or a part of a protein which is desired to be expressed in Caulobacter and which may be secreted by the bacterium. The heterologous polypeptide includes enzymes and other functional sequences of amino acids as well as ligands, antigens, antigenic epitopes and haptens. The size of the heterologous polypeptide will be selected depending upon whether an intact S-layer is to be produced in the Caulobacter or whether the chimeric protein to be recovered from the bacterial medium as described below. Preferably, the cysteine content of the heterologous polypeptide and the capacity for formation of disulphide bonds within the chimeric protein will be kept to a minimum to minimize disruption of the secretion of the chimeric protein.

[0030] Once a particular bacterium's S-layer protein gene is characterized, this invention may be practised by implementing one or more known methods to clone a selected heterologous coding sequence into all or part of the S-layer protein gene so that both the S-layer protein and the heterologous sequence are transcribed “in-frame”. Knowledge of an S-layer protein gene sequence permits one to identify potential sites to install the heterologous genetic material. The repetitive nature of the protein in the S-layer permits multiple copies of a heterologous polypeptide to be presented on the surface of the cell.

[0031] The following general procedure lays out courses of action and specifies particular plasmid vectors or constructions that may be used to accomplish fusion of an S-Layer protein with a polypeptide of interest. The following description uses the rsaA (S-layer) gene of C. crescentus as an example (see FIG. 6 and SEQ ID NO:6). The latter gene sequence is characterized in Gilchrist, A. et al (1992) [supra).

[0032] The general procedure includes detailed steps allowing for the following possibilities:

[0033] 1) use of a collection of potentially permissive sites in the S-layer gene to install the genetic information for a polypeptide of interest;

[0034] 2) use of a Carrier cassette for delivering a gene of interest to sites within the S-layer gene (the cassette offers several advantages over direct modification of a gene of interest, in preparation for insertion);

[0035] 3) creation of a collection of random insertion sites based on a restriction enzyme of choice, if the available collection of potentially permissive sites is for some reason unsuitable; and,

[0036] 4) preparation of DNA coding for a polypeptide of interest for direct insertion into permissive sites (ie, not using the Carrier cassette) by a method best suited for the particular case (several options are suggested).

[0037] The general procedure involves the following steps and alternative courses of action. As a first step the practitioner will choose an appropriate region (or specific amino acid position) of the S-layer for insertion of a desired polypeptide. Second, the practitioner will create a unique restriction site (preferably hexameric) in the rsaA (S-layer) gene at a position within the gene encoding that region (or corresponding to a specific amino acid) using either standard linker mutagenesis (regional) or site directed mutagenesis (specific amino acid). The unique restriction site will act as a site for accepting DNA encoding the polypeptide of interest. The plasmid-based promoter-less version of the rsaA gene (pTZ18U:rsaAΔP) shown in FIG. 2 may be used because it contains an appropriate combination of 5′ and 3′ restriction sites useful for subsequent steps (see: Gilchrist, A. et al (1992) [supra]). The restriction site should not occur in rsaA, its carrier plasmid or the DNA sequence coding for the polypeptide of interest.

[0038] If it is unclear which region of the S-layer would be suitable for insertion of a polypeptide of interest, a random linker mutagenesis approach is used to randomly insert a unique linker-encoded restriction site (preferably hexameric) at various positions in the rsaA gene. Sites for insertion of the linker are created using an endonuclease, either of a sequence specific nature (e.g. tetrameric recognition site restriction enzyme) or sequence non-specific nature (e.g. Deoxyribonuclease I [DNase I]). A particularly suitable method is the generalized selectable linker mutagenesis approach based on any desired restriction site of: Bingle, W. H., and J. Smit. 1991 “Linker Mutagenesis Using a Selectable Marker: A Method for Tagging Specific Purpose Linkers With an Antibiotic-Resistance Gene”. Biotechniques 10: 150-152. Because endonuclease digestion is carried out under partial digestion conditions, a library of linker insertions at different positions in rsaA is created. Partial digestion with MspI, HinPI and Aci:I can create 150 potential sites for insertion of a Bam HI linker such as:

[0039] 5′-CGACGGATCCGT

[0040] TGCCTAGGCAGC-5′

[0041] (SEQ ID. NO:10).

[0042] If restriction endonucleases are used to create sites for subsequent insertion of a linker encoding a hexameric restriction site, mutagenesis may also be done with a mixture of 3 different linkers incorporating appropriate spacer nucleotides in order to satisfy reading frame considerations at a particular restriction site (only 1 of the 3 linker insertions will be useful for subsequent acceptance of DNA encoding the polypeptide of interest). With DNase I, only one linker is needed, but again only 1 of 3 linker insertions may be useful for accepting DNA encoding the polypeptide of interest depending on the position of the DNase I cleavage with respect to the 3 bases of each amino acid codon.

[0043] Next, a linker tagged with a marker is used to insert DNA of interest at a restriction site. For example, if BamHI sites are appropriate as sites for the introduction of DNA encoding a polypeptide of interest, BamHI linkers tagged with a kanamycin-resistance gene for selectable linker mutagenesis may be used. One such 12-bp linker carried in plasmid pUC1021K was described by Bingle and Smit (1991) [Supra]. Two additional 15-bp linkers (pUC7165K and pTZ6571K) constructed for creating the other 2 possible translation frames within the linker insert itself are described in FIGS. 3 and 4 (SEQ ID NO:2; SEQ ID NO:3; SEQ ID NO:4; and, SEQ ID NO:5). Any one of the above three kanamycin-resistance tagged BamHI linkers is suitable for mutagenesis at sites created in rsaA by DNase I. As outlined above, a mixture of all three linkers is preferably used for mutagenesis at sites created in rsaA by restriction enzyme digestion.

[0044] Once a library composed of linker insertions encoding desired hexameric restriction site at different positions in rsaA has been created, the DNA encoding a polypeptide of interest is inserted into the sites en masse (the library of mutated rsaA genes may be manipulated as one unit). The library is digested with the restriction enzyme specific for the newly-introduced linker encoded restriction site and ligated to a DNA fragment encoding the polypeptide of interest and carrying the appropriate complementary cohesive termini. The DNA specifying the polypeptide of interest can be prepared by a number of standard methods, which may include oligonucleotide synthesis of 2 anti-complementary strands, polymerase chain reaction (PCR) procedures, or addition of linkers whose termini are compatible with the introduced sites in rsaA to a suitably modified segment of DNA.

[0045] In order to facilitate the rapid recovery of useful rsaA genes carrying newly inserted DNA at BamHI sites encoding the polypeptide of interest, the Carrier oligonucleotide shown in FIG. 1 may be used. The Carrier is designed to accept DNA (including multiple copies and mixtures) prepared by PCR or annealed synthesized oligonucleotides and controls direction of insertion of the foreign segment into a rsaA gene through use of a promoterless drug resistance marker. The DNA of interest is first directionally cloned, if possible, using the XhoI, StuI, or SalI sites or non-directionally cloned using any one of the sites in the same orientation as a promoterless chloramphenicol resistance (CmR) gene. To do this the DNA of interest must be provided with the appropriate termini for cloning and spacer nucleotides for maintaining correct reading frame within the cassette and should not contain a BglII site. For insertion into the BamHI linker library, the DNA of interest is recovered as a BamHI fragment tagged with a CmR gene. When ligated to the BamHI digested rsaA linker library, only those colonies of the bacterium (eg. E. coli) used for the gene modification steps that are recovered will be those carrying insertions of the desired DNA in the correct orientation, since the promoter on the plasmid is 5′ to rsaAΔP and the CmR gene. This eliminates screening for DNA introduction and increases the recovery of useful clones by 100% (1 of 3 versus 1 of 6). While still manipulating the library as one unit, the CmR gene is removed using BglII. The carrier oligonucleotide also provides the opportunity to add DNA 5′ or 3′ to the DNA of interest at SalI, XhoI or StuI sites providing the DNA of interest does not contain any of these sites. This allows some control over spacing between rsaA sequences and the sequence of the DNA of interest.

[0046] Next, the rsaA genes carrying the DNA of interest in the correct orientation is excised from the plasmid (eg. from the pTZ18U:rsaAΔP plasmid) and is transferred to a suitable vector providing a promoter recognized by Caulobacter. Such vectors include pWB9 or pWB10 (as described in Bingle, W. H., and J. Smit. 1990). “High Level Plasmid Expression Vectors for Caulobacter crescentus Incorporating the Transcription and Transcription-Translation Initiation Regions of the Paracrystalline Surface Layer Protein Gene”. Plasmid 24: 143-148) with EcoRI/SstI sites. The DNA of interest should not contain the same restriction sites present in the vector. The latter vectors allow expression of rsaA hybrids in S-layer negative mutants of C. crescentus such as CB15KASac.

[0047] Those Caulobacter surviving transfer are examined for chimeric protein secretion, S-layer assembly and presentation of the new polypeptide activity, antigenicity, etc. by methods specific to the needs of the investigator or the capabilities of the inserted sequence. Many of the sites created are “benign” as they have no effect on the functional regions of the protein involved with export, self assembly, etc. However, not every site that results in an absence of functional disruption of the S-layer is best for insertion of new activities. Some sites may not be well exposed on the surface of the organism and other sites may not tolerate insertion of much more DNA than the linker sequence.

[0048] By selecting the site of insertion of the heterologous material, it is possible to express heterologous polypeptides of up to about 60 (preferably less than 50) amino acids in a rsaA chimeric protein which will assemble as an S-layer on the cell surface. Single or multiple insertions of smaller polypeptides (eg. 10-20 amino acids) at a wide range of the permissive sites in rsaA will permit S-layer formation. Some sites, as reported herein, are sensitive to even small insertions resulting in the chimeric protein being released into the medium. Release may also be deliberately effected by use of a shedding strain of Caulobacter to express the chimeric protein or by physical removal of the S-layer from whole cells.

[0049] Where S-layer formation is not required, this invention permits the expression of quite large polypeptides (eg. about 200 amino acids) as part of rsaA protein. Expressing a chimeric protein containing a rsaA component having substantial deletions, as described below, may increase the size of the heterologous polypeptides that will be expressed and secreted by Caulobacter.

[0050] The preceding methods describe insertion of linkers in-frame into an rsaA gene (eg. a promoterless version of the gene). The sites that are introduced allow subsequent insertion of foreign DNA in-frame into the full length rsaA gene. This invention also includes the construction of chimeric rsaA genes and the resulting production of chimeric rsaA protein wherein the rsaA gene component is highly modified by deleting large portions of the rsaA gene which reduces the amount of Caulobacter protein present in the secreted chimeric protein.

[0051] Generally, large deletions throughout the rsaA gene will result in a chimeric protein that is not capable of forming an S-layer. Attachment of the S-layer to the cell is abolished if about the first 29 N-terminal amino acids of rsaA are deleted. Deletion of the first 776 amino acids from the N-terminal of rsaA will still result in a chimeric protein that is secreted from the cell but having a rsaA component of only the 250 C-terminal amino acids. It has also been found that only the extreme C-terminal region corresponding to approximately amino acids 944-1026 of rsaA is required for secretion of an rsaA chimeric protein from Caulobacter. Thus the chimeric protein need only have the rsaA C-terminal region to be secreted from the cell. Furthermore, use of the C-terminal region of rsaA of about amino acids 850-1026 (or more) not only permits the cell to transport the chimeric protein outside of the cell, but also promotes spontaneous aggregation of much of the secreted chimeric protein in the cell medium and formation of a macroscopic precipitate that may be collected with a course mesh or sheared to micron-sized particles which may be ideal for vaccine presentation. Yields of up to 250 mg. (dry weight) of protein per liter of cells may be possible.

[0052] This invention may be practised as shown in the Examples by expression of modified rsaA genes borne on plasmids that are broad host range vectors capable of being expressed in Caulobacter. Such plasmids are readily constructed and introduced to Caulobacter by electroportation. Typically, the plasmid is maintained in the Caulobacter by antibiotic selection. Highly modified rsaA genes with attached heterologous sequences may also be introduced into Caulobacter on a plasmid that is not replicated by Caulobacter. At a low but practicable frequency, homologous recombination of the incoming modified rsaA gene with the chromosome-resident copy of rsaA in the cell will result in a gene rescue or transfer event. In some cases it may be desirable to obtain a stable cell line in which the chimeric rsaA gene is chromosomal. Various protocols for creating chromosomal insertions are set out in the Examples.

[0053] Use of the S-layer protein as a vehicle for production of a heterologous polypeptide has several advantages. Firstly, the S-layer protein is synthesized in large quantities and has a generally repetitive sequence. This permits the development of systems for synthesis of a relatively large amount of heterologous material as a fusion product with an S-layer protein (chimeric protein). It may be desirable to retain the chimeric protein as part of the bacterial cell envelope or, the fusion product may be separated from the organism, such as by the method described in: Walker, S. G., et al. 1992. “Isolation and Comparison of the Paracrystalline Surface Layer Proteins of Freshwater Caulobacters”. J. Bacteriol. 174:1783-1792. Alternatively, the Caulobacter strain that is used to express the fusion product may be derived from a strain such as CB15Ca5 that sheds its S-layer.

[0054] This invention is particularly suited for use in a bioreactor systems. An example would be the use of a modified Caulobacter expressing a polypeptide having activity similar to that of a metallothionein in a bioreactor, to bind toxic metals in sewage, waste water etc. Caulobacters are ideal candidates for fixed-cell bioreactors, the construction of which is well known. An example of such a bioreactor is a rotating biological contactor. Although other bacteria are found in the environment that are capable of binding metals, they often do so by producing copious polysaccharide slimes that quickly plug filtration systems. In some cases, the bacteria are not surface-adherent or the bacteria do not show selectivity towards key toxic metals. By taking advantage of the natural bio-film forming characteristics of Caulobacter, bioreactors may be formed comprising a substrate and a single layer of cells adhered thereon, with the cells distributed at high density. A variety of substrates may be used such as a column of chemically derivatized glass beads or a porous ceramic material such as ceramic foam.

[0055] Another advantageous application for this invention is in the production of batch cultures of modified Caulobacter wherein the S-layer protein is a fusion product with an enzyme. For example, such Caulobacter could be grown in wood pulp suspensions at an appropriate juncture of the pulping process in order to provide for enzymatic decomposition of the wood-pulp structure (e.g. with an enzyme having an activity like xylanase or cellulase). Such an application may permit more effective penetration of bleaching agents in the wood-pulp bleaching process thereby reducing the use of chlorine-based bleaching agents.

[0056] Examples of enzymes that may be expressed as chimeric rsaA proteins include alkaline phosphatase (eg. by expression of the pho A gene of E. coli; see: Hoffman, C. S., and Wright, A. 1985. “Fusions of Secreted Protein to Alkaline Phosphatase: An Approach for Studying Protein Secretion”. Proc. Natl. Acad. Sci. U.S.A. 82:5107-5111; Bingle, W. H., et al. 1993.” An “All Purpose” Cellulase Reporter for Gene Fusion Studies and Application to the Paracrystalline Surface (S)-Layer Protein of Caulobacter crescentus”. Can.J. Microbiol.39: 70-80; and Bingle, W. H. and Smit, J. 1994. “Alkaline Phosphatase and a Cellulase Reporter Protein Are Not Exported From the Cytoplasm When Fused to Large N-terminal Portions of the Caulobacter crescentus Surface (S)-Layer Protein”. Can.J. Microbiol. 40:777-782.) and, cellulase (eg. by expression of the CenA gene of Cellulomonas fimi; see: Bingle, W. H. et al. (1993) [supra]; and Bingle, W. H. and Smit, J. (1994) [supra]).

[0057] Another advantageous application of this invention is the production of organisms that secrete and optionally present vaccine-candidate epitopes. For example, modified Caulobacter may be readily cultured in outdoor freshwater environments and would be particularly useful in fish vaccines. The two-dimensional crystalline array of the S-protein layer of Caulobacter, which has a geometrically regular, repetitive structure, provides an ideal means for dense packing and presentation of a foreign epitope to an immune system in cases where the epitope is part of an intact S-layer in the bacterial cell surface.

[0058] This invention also provides an efficient expression system for polypeptides that may be harvested in large quantities relatively free of contaminants and protein of Caulobacter origin. Expression of a heterologous polypeptide fused with sufficient C-terminal amino acids of the rsaA protein to promote secretion of the heterologous polypeptide results in the accumulation of large quantities of secreted protein in the cell medium. In such cases, the chimeric protein does not have to be released from the cell surface. Furthermore, adjustment of the size of the N-terminal rsaA portion can dictate whether the secreted protein is soluble or will precipitate in the cell medium. This embodiment may also be useful in cases where the Caulobacter is to express a foreign antigenic component and it is desired to minimize the amount of Caulobacter protein that is associated with the foreign antigen secreted by the Caulobacter.

EXAMPLE 1 Production of Permissive Insertion Sites in C.crescentus

[0059] Using the restriction enzyme TaqI, a partial digestion of the rsaA gene in pTZ18U:rsaAΔP produced a group of linearized segments with random TaqI sites cleaved. The linearized segments were modified by use of the tagged linker mutagenesis procedure of Bingle and Smit (1991) [supra], using the 12-bp BamHI linker carried in plasmid pUC102K discussed in the general procedure above. Those products that produced a full-length protein in E. coli were ultimately transferred to pWBI (a minor variation of pWB9 that is replicated by Caulobacter), as described in the general procedure. The resulting construction was introduced into a C. crescentus strain. Distinguishable events were retrieved and analyzed for the ability to produce a full-length protein in C. crescentus and to produce the crystalline S-layer on their surface and the approximate location of the insertion. Cells were screened for the presence of a S-layer protein of approximately 100 kDa that is extracted from the surface of whole cells by 100 mM HEPES at ph2. The results of this screening together with the approximate positions of five successful events (and subsequently determined exact or specific insertion positions) are illustrated in FIG. 5.

[0060] The above-described five positive events represent cases where the 4-amino acid insertion is tolerated with no effect on the S-layer function. The S-layers of the modified Caulobacter were indistinguishable from a wild-type S-layer. Thus, they have a higher potential for tolerating the addition of more foreign peptide material than less characterized sites. By producing 3 versions of the gene of interest, representing each possible reading frame (using standard linker addition technology), one may test each of these sites for suitability in expressing the desired activity. Also, by using restriction enzymes other than TaqI (such as AciI, HinPI or MspI) a larger library of BamHI insertions may be created.

EXAMPLE 2 Insertion of Cadmium Binding Polypeptides into Specific Sites

[0061] An insertion of the above described 12 bp linker was made at the TaqI site that corresponds to amino acid #188, frame #3 (see FIG. 6; SEQ ID NO:6; and, SEQ ID NO:7). This created a unique BamHI site at that position. Because the precise position of the TaqI site could be assessed from the DNA sequence information available for the rsaA gene, the necessary translation frame was known and thus a single construction of a metallothionein gene was made. This was done by excision of the coding sequence of monkey metallothionein II peptide (60 amino acids comprising 10 cysteine residues and having a molecular weight of about 5000) at known restriction sites and adapting the gene ends with BamHI linkers with appropriate base pair spacers for the needed translation frame.

[0062] After insertion into the BamHI site created at position 188, frame 3, several clones were examined by determining whether they could bind elevated levels of cadmium by the assay described below. The assay was necessary because the segment had equal probability of being inserted backwards. One clone that gave positive results was examined by electron microscopy and the presence of a normal S-layer was confirmed. The plasmid in the clone that gave positive results was also examined by DNA sequencing analysis, sequencing across the junction between the position 188 site and the 5′ side of the metallothionein gene. The sequence data confirmed correct orientation.

[0063] The plasmid-containing clone and relevant control strains were examined for the ability to bind several metals known to be bound by native metallothionein. This was done by growing the strains of bacteria in the presence of the metals at a concentration of 5 ug/ml. After extensive washing of the cells to remove unbound metal, the cells were ashed by treatment at 500° C. and the residue was dissolved in dilute nitric acid and examined for metal content by atomic absorption spectroscopy. The results from one round of data collection is shown in Table 1. In the case of cadmium and copper, an elevated level of bound metal is noted in the metallothionein-expressing strains. TABLE 1 Metal Ion Tested (ug/metal/OD unit of cells Copper Trial Caulobacter 1 2 Cadmium Zinc CB15 1.79 1.0 0.71 4.15 (wild-type, S-layer[+]) CB15XSAC 2.18 1.33 1.07 4.08 (S-layer negative strain) CB15ESAC/p188.3 2.01 1.30 11.1 3.66 (contains S-layer with linker insert only) CB15KSAC/p188.31a 2.79 3.09 19.1 3.00 (S-layer with Metallotbionein inserted)

EXAMPLE 3 Investigation of Other Permissive Sites in rsaA Gene

[0064] A library of 240 BamHI linker insertions was created using the procedures of Example 1. Of the 240 insertions, 45 target sites in the rsaA gene were made with TaqI. 34 of the latter insertions were discarded because the clones contained deletions of rsaA DNA as well as the linker insertions. The remaining 11 resulted in 5 non-permissive and the 6 permissive sites described in Example 1. The remaining 195 insertions in the library were made using the enzymes HinPI, AciI, and MspI to create target sites as outlined in Example 1. Of the latter 195 insertions, 49 permissive sites were located for a total of 55. Of those sites scored as non-permissive, some may have had deletions of rsaA DNA at the linker insertion site. One BamHI linker insertion at a TaqI site thought to be permissive was later found by nucleotide sequencing to be located outside the rsaA structural gene reducing the total number of permissive sites to 54 from 55.

[0065]FIG. 7 illustrates the approximate location by restriction mapping of 54 permissive sites. The results show that sites that will accept 2-4 amino acids while still allowing the protein to be made and assembled into an S-layer are scattered up and down the protein. Furthermore, there is an unexpectedly high proportion of sites at which such insertions do not prevent expression and assembly of the S-layer. The results indicate that approximately 25-50% of in-frame linker insertions will be tolerated by the S-layer protein and the Caulobacter and that diverse regions of the protein will tolerate insertions. Thus, Caulobacter is an ideal candidate for expression of polypeptides fused with the S-layer and the presence of multiple permissive sites extending along the rsaA gene will permit the insertion of a plurality of the same or different peptides into the same rsaA protein molecule and expressed on the surface of a single Caulobacter.

EXAMPLE 4 Further Studies with Cadmium Binding Polypeptides

[0066] The results described for Example 3 indicated that it would be possible to insert metallothionein at multiple places in the rsaA protein and thereby enhance the metal binding capacity of such a transformed Caulobacter. However, when the procedures of Example 2 were repeated to insert the metallothionein coding sequence into others of the 54 permissive sites identified in the preceding Example in each case, the transformed Caulobacter did not secrete a chimeric protein and did not synthesize an S-layer. Furthermore, the transformed Caulobacter of Example 2 was stable as long as the transformants were frozen immediately after isolation. When continuously cultured for approximately one week, the transformants deleted the metallothionein portion of the S-layer and the S-layer protein returns to its normal size.

[0067] Consideration of the predicted amino acid sequence of the rsaA protein shows that the latter protein lacks cysteine residues whereas metallothionein has a high cysteine content. It thus appeared that for secretion and long term expression of a rsaA chimeric protein, the heterologous polypeptide portions of the chimeric protein should not have high cysteine content and preferably, not be capable of forming multiple disulphide bonds in the chimeric protein in an aerobic environment.

[0068] Following the foregoing procedures, single and multiple copies of DNA encoding the synthetic cadmium binding peptide shown in FIG. 10 (SEQ ID NO:11) was synthesized, inserted at amino acid 277 of rsaA using the above described Carrier cassette and was expressed in C. crescentus. The peptide has a single cysteine residue. Mild acid extracts of whole cells expressing the modified rsaA gene were subjected to SDS-PAGE for identification of S-layer proteins. The S-layer protein was expressed and secreted when there was from 1 to 3 copies of the cadmium binding peptide present at rsaA amino acid position 277. Insertion of 4 or more copies resulted in a dramatic reduction of S-layer protein released from the whole cells by mild acid treatment to barely detectable levels. Detection by autoradiography of rsaA protein in vivo labelled with 35 S-cysteine and in vitro with 125 I-iodoacetamide confirmed that the cadmium binding peptide was part of the chimeric rsaA protein. This demonstrates that Caulobacter crescentus is capable of secretion of a chimeric rsaA protein having a limited cysteine content and a limited capacity for disulphide bond formation within the chimeric protein.

EXAMPLE 5 Expression and Presentation of Antigenic Epitopes on Caulobacter Cell Surface

[0069] Using the library of the 49 permissive sites other than those made with TaqI described in Example 3, the coding sequence for a 12-amino acid pilus peptide epitope lacking cysteine residues from Pseudomonas aeruginosa PAK pilin was inserted at the sites using the procedures described above and employing the Carrier cassette shown in FIG. 1. Positioning of the added DNA between the first Bam HI site and the Bg III site permitted use of the latter site for making repeated insertions of DNA.

[0070] The pilus epitope DNA shown in FIG. 8 (SEQ ID NO:8) codes for the amino acids numbered 1-12 in superscript and was prepared by oligonucleotide synthesis of two anti-complementary strands. The transformed bacteria were screened for both production and presentation of the epitopes by the transformed Caulobacter by using standard Western immunoblot analysis (see: Burnette, W. N. 1981. “Western Blotting; Electrophoretic Transfer of Protein from Sodium Dodecyl-Polyacrylamide Gels to Unmodified Nitrocellulose and Radiographic Detection Antibody and Radioiodinated Protein A”. Analytical Biochemistry 112:195-203) and by colony immunoblot tests in which the cells were not disrupted (see: Engleberg, N. C., et al. 1984. “Cloning an Expression of Legionella pneumophilia Antigens in Escherichia coli”. Infection and Immunity 44:222-227). Anti-pilus monoclonal antibody obtained from Dr. Irvin, Dept. of Microbiology, University of Alberta (Canada) was used in the immunoblot analyses to detect the presence of the pilus epitope insert. The antibody (called PK99H) was prepared using purified Pseudomonas aeruginosa PAK pilin as the antigen and the monoclonal antibody against the 12 amino acid epitope was isolated by standard techniques using BALB/C mice as a source of ascites fluid. Reaction with the antibody in the whole cell colony immunoblot assay shows that the epitope is not only expressed in the transformed Caulobacter but is exposed on the S-layer surface overlying the cell in such a way that the epitope is available to the antibody.

[0071] Of the organisms screened, insertions of the pilus epitope at the following sites in the rsaA gene as determined by nucleotide sequencing resulted in a positive reaction with the antibody in the whole cell Colony immunoblot analysis: 69, 277, 353, 450, 485, 467, 551, 574, 622, 690, 723, and 944. The results show that the permissive sites that will accept polypeptides of the size of the pilus epitope are numerous and scattered across the rsaA gene.

[0072] Further studies with the pilus peptide resulted in successful expression and secretion of rsaA chimeric proteins have single copies of the peptide at the locations shown in FIG. 11. Also, four and seven copies of the pilus peptide were expressed and secreted as a rsaA chimeric protein when inserted at amino acids 277 and 551 respectively of the rsaA protein. However, insertions of the pilus peptide at amino acids 69, 277, 450, 551 and 622 resulted in a chimeric protein that did not attach to the cell surface and was released into the culture medium.

EXAMPLE 6 Insertion of Large Polypeptides

[0073] Bacterial surface proteins from organisms other than Caulobacter described in the prior art are generally not known to accept polypeptides larger than about 60 amino acids within the structure of the surface protein. The procedures of the preceding Example were carried out in order to insert the coding sequence of a 109 amino acid epitope from IHNV virus coat glycoprotein at insertion sites identified in the preceding Example. The IHNV epitope was prepared by PCR and had the portion of the sequence shown in FIG. 9 (SEQ ID NO:9) which is equivalent to amino acid residues 336-444 of the IHNV sequence described in: Koener, J. F. et al. 1987. “Nucleotide Sequence of a cDNA Clone Carrying the Glycoprotein Gene of Infectious Hematopoietic Necrosis Virus, a Fish Rhabdovirus”. Journal of Virology 61:1342-1349. Anti-IHNV polyclonal antibody against whole IHNV obtained from Dr. Joann Leong, Dept. of Microbiology, Oregon State University, U.S.A. (see: Xu, L. et al. 1991. “Epitope Mapping and Characterization of the Infectious Hematopoietic Necrosis Virus Glycoprotein, Using Fusion Proteins Synthesized in Escherichia coli”. Journal of Virology 65:1611-1615) was used in the immunoblot assays described in the preceding Example to screen for Caulobacter that express and present the IHNV sequence on the surface of the S-layer of the Caulobacter. Reaction in the whole cell colony immunoblot assay was positive in respect of insertions at sites 450 and 551, and negative at a site which was at approximately amino acid 585.

[0074] The IHNV insert contains a single cysteine residue and is an extremely large insert for successful expression as a fusion product with a bacterial surface protein.

[0075] In further studies, the same 109 amino acid portion of the IHNV glycoprotein was inserted at amino acid 450 of rsaA. The chimeric protein expressed and secreted by Caulobacter crescentus and was recovered from the cell culture medium. SDS-PAGE analysis of the recovered proteins showed that some of the chimeric proteins were smaller than the predicted rsaA chimeric protein but still bound anti-IHNV antibody. Analysis of these proteolytic products showed that cleavage of the chimeric protein occurred at an Arg residue encoded by the gene transfer cassette shown in FIG. 1. Thus in some cases, adjustment of the nucleotide sequence at the interface of the polypeptide and rsaA coding sequences may be necessary to prevent expression of an arginine residue.

EXAMPLE 7

[0076] Methods are described above for the insertion of 12-bp BamHI linker sites into a promoterless version of the rsaA gene. Because linker insertions involve the insertion of 12 bp (i.e. a multiple of three) an in-frame linker insertion resulted in every case. These linker sites are introduced to allow subsequent insertion of DNA encoding foreign peptide/proteins. Expression of such chimeric genes leads to the production of an entire full-length rsaA protein carrying the inserted heterologous amino acid sequence of interest. A number of BamHI site positions were identified above precisely by nucleotide sequencing. Four of the sites in the rsaA gene correspond to amino acid positions 188, 782, 905, 944 in the rsaA protein. For this example, an additional linker insertion was created at amino acid position 95 of the native gene (i.e. this gene carried its own promoter) using the same methodology. All five in-frame BamHI linker insertion sites were inserted in the rsaA so that the nucleotides of the linker DNA were read in the reading frame GGA/TCC (FIG. 12).

[0077] Because all BamHI linker nucleotides were read in the same reading frame, the 5′ region of one rsaA gene carrying a BamHI linker insertion at one position could be combined with the 3′ region of an rsaA gene carrying another of the BamHI linker insertions to create in-frame deletions with a BamHI site at the joint between adjacent regions of rsaA. Using such a method, in-frame deletions of rsaA (ΔAA95-782) and rsaA(ΔAA188-782) were created.

[0078] DNA fragments encoding various C-terminal portions of the 1026 amino acid rsaA protein were isolated using the newly inserted BamHI linker sites as the 5′-terminus of the fragment and a HindIII site as the 3′ terminus of the fragment. These BamHI fragments were transferred to the BamHI/HindIII sites of pUC8 (J. Vieira, and J. Messing. 1982.” The pUC Plasmids, an M13mp7-Derived System for Insertion Mutagenesis and Sequencing With Synthetic Universal Primers” Gene 19:259-268) creating “rsaA C-terminal Segment Carrier plasmids” (FIG. 12). The insertion into pUC8 also resulted in the creation of an in-frame fusion between the first 10 N-terminal amino acids of LacZa and the various C-terminal fragments (AA782-1026, AA905-1026 or AA944-1026) of rsaA. These LacZa:rsaA fusion proteins can be produced in C. crescentus using the lacZa transcription/translation initiation signals when introduced on appropriate plasmid vectors or direct insertion into the chromosome (see: W. H. Bingle, et al. 1993. “An All-Purpose Cellulase Reporter for Gene Fusion Studies and Application to the Paracrystalline Surface (S)-Layer Protein of Caulobacter crescentus.” Can. J. Microbiol. 39:70-80).

[0079] Both types of constructions (i.e., the deletion versions and the C-terminal only segments) result in the production of proteins that are secreted in Caulobacter strains as highly modified rsaA proteins. The gene segments can also facilitate the secretion of heterologous polypeptides by insertion or fusion of appropriate DNA sequences at the unique BamH1 site that exists in each of the constructions. The following describes specific methods for doing so to create chimeric proteins capable of secretion in C. crescentus.

[0080] A—Creating fusions of desired sequences with C-terminal portions of rsaA—Method 1

[0081] The general process is as follows:

[0082] 1) Inserting the desired sequence into the Carrier cassette.

[0083] The following describes the specific manner in which heterologous sequences may be introduced into the Carrier cassette of FIG. 1.

[0084] a) Insertion of a single copy of the desired gene segment.

[0085] Depending upon the length of the gene segment, two methods of construction may be used. For segments of up to about 30 amino acids, two oligonucleotides of appropriate sequence are chemically synthesized, annealed by mixing, heating and slow cooling and then ligated into the Carrier cassette. The oligonucleotides will also contain additional base pairs that recreate “sticky ends” of appropriate restriction endonuclease sites at each end of the duplex DNA that results from the annealing process.

[0086] For longer segments, PCR is used to amplify a region of a target DNA sequence. Oligonucleotides are synthesized that have sequence complementary to the boundaries of the desired sequence and which contain additional base pairs that recreate a “sticky end” of an appropriate restriction endonuclease site. In the present example oligonucleotides are made to produce products with the appropriate restriction endonuclease site for directional cloning into the Carrier cassette. PCR amplification of the desired sequence is then done by standard methods.

[0087] For both methods, the sticky ends prepared must be appropriate for an XhoI site at the 5′ terminus of the desired DNA sequence and StuI or SalI sites at the 3′ terminus; this places the desired gene segment in the correct orientation within the Carrier cassette. Reading frame continuity is maintained by appropriate design of the oligonucleotides used for the PCR step.

[0088] b) Preparation of multiple copies of the desired gene segment.

[0089] The Carrier cassette also allows production of multiple insert copies. A BglII site in the cassette is restored after removal of the promoterless antibiotic resistance gene; that site can be used to insert an additional copy of the Carrier/desired sequence insertion, using the terminal BamHI sites, because the “sticky ends” produced by both BamHI and BglII are the same. This “piggy-back” insertion still maintains the correct reading frame throughout the construction. Any number of additional cycles of “piggy-backing” can be done because the BamHI/BglII ligation results in sequence which is no longer a substrate for either enzyme. The result is the production of cassettes of multiple copies of the desired sequence which can be transferred to appropriately modified rsaA genes with the same ease as a single copy. An additional intrinsic feature of this method is that different heterologous sequences can be paired together in this multiple copy cassette with the same ease as multiple copies of the same heterologous sequence.

[0090] Example 7a. Insertion of an 109 amino acid segment of the IHNV surface glycoprotein to Carrier cassette.

[0091] Using the methods described, a PCR product was made that contained the DNA coding for amino acids 336 to 444 (FIG. 9) of the major surface glycoprotein of the Infectious Hematopoietic Necrosis Virus (IHNV), which infects Salmonid fish.

[0092] Example 7b. Insertion of an 184 amino acid segment of the IHNV surface glycoprotein to Carrier cassette.

[0093] Using the methods described a PCR product was made that contained the DNA coding for amino acids 270 to 453 of the IHNV glycoprotein segment shown in FIG. 9..

[0094] Example 7c. Insertion of single and multiple copies and an epitope of the Pseudomonas aeruginosa PAK pilus gene to Carrier cassette.

[0095] Oligonucleotides were constructed to code for the pilus epitope described in Example 5, which corresponds to a sequence at the extreme C-terminus of the pilus protein. Using the methods outlined in part A(1) (b) of this Example, 3 tandem copies were prepared.

[0096] 2) Transfer of Carrier cassette to the rsaA C-terminal Segment Carrier plasmids.

[0097] The constructions described in examples 7a and 7b above are then transferred to the rsaA C-terminal Segment Carrier plasmids, described above, resulting in an in-frame fusion of: a) a very short section of the betagalactosidase protein (10 amino acids), b) the desired sequence flanked by 2-3 amino acids derived from Carrier cassette sequence and c) the appropriate rsaA C-terminal segment.

[0098] Example 7d. Fusion of Carrier/109 AA and 184 IHNV segments to C-terminal rsaA segment AA782-1026.

[0099] This was done using the Carrier cassettes described in Examples 7a and 7b above and the AA782-1026 rsaA C-terminal Segment Carrier plasmid described above.

[0100] Example 7e. Fusion of Carrier/109 AA and 184 AA IHNV segments to C-terminal rsaA segment AA905-1026.

[0101] This was done using the Carrier cassettes described in Examples 7a and 7b above and the AA905-1026 rsaA C-terminal Segment Carrier plasmid described above.

[0102] Example 7f. Fusion of Carrier/109 AA and 184 AA IHNV segments to C-terminal rsaA segment AA944-1026.

[0103] This was done using the Carrier cassettes described in Examples 7a and 7b above and the AA944-1026 rsaA C-terminal Segment Carrier plasmid described above.

[0104] Example 7g. Fusion of Carrier/3× Pilus Epitope segment to C-terminal rsaA segment AA782-1026.

[0105] This was done using the Carrier cassettes described in Example 7c above and the AA782-1026 rsaA C-terminal Segment Carrier plasmid described above.

[0106] 3) Expression of the desired fusion in an appropriate C. crescentus host strain.

[0107] a) Plasmid-based expression.

[0108] To create plasmid vectors that can be introduced and maintained in appropriate C. crescentus strains, the entire rsaA C-terminal Segment Carrier plasmids were fused to broad host range vectors pKT215 or pKT210 (see: M. Bagdasarian, et al. 1981.” Specific-Purpose Cloning Vectors. II. Broad-Host-Range, High Copy Number RSF1010-Derived Vectors, and a Host-Vector System for Gene Cloning in Pseudomonas.” Gene 16:237-247) using the unique HindIII restriction site present in each plasmid. The resulting plasmid is introduced into Caulobacter by conjugation or electroporation methods and is maintained by appropriate antibiotic selection.

[0109] The fusions described in examples 7d-7g were expressed in Caulobacter. In each case expression and secretion of the chimeric rsaA protein was detected by Western immunoblot analysis of electrophoretic gels of the cell culture supermutant employing the monoclonal antibody for each of the polypeptide epitopes. The transporter signal for secretion from Caulobacter must be in the C-terminal region of amino acids 944-1026 of rsaA protein as all chimeric proteins in the examples were secreted. Precipitation of the chimeric protein occurred with the use of rsaA segment AA782-1026 but not AA944-1026. Recovery of precipitate using AA905-1026 was reduced as compared to AA782-1026.

[0110] b) Selection of appropriate C. crescentus host strains

[0111] In nearly all cases the use of an rsaA-negative C. crescentus host strain is appropriate. C. crescentus strain CB2A and strain CB15aKSac fulfil this requirement. If it is important to ensure that all fusion protein is no longer attached to the cell surface, the use C. crescentus strains CB15Ca5KSac or CB15Ca10KSac are appropriate. These strains have additional mutations that result in the loss of the production of a specific species of surface lipopolysaccharide that is has been demonstrated to be involved with the surface attachment of native rsaA protein as a 2-dimensional crystalline array (see: Walker S. G. et al 1994. “Characterization of Mutants of C. crescentus Defective in Surface Attachment of the Paracrystalline Surface Layer”. J. Bacteriol. 176:6312-6323). Most often with the highly modified versions of the rsaA gene, this precaution is not necessary since virtually all regions of the gene that may have a role in the attachment process have been removed.

[0112] There are two types of growth media well suited to both propagation of Caulobacter for general purposes, including cloning steps, and also to produce the secreted and aggregated chimeric proteins. Example of the two types are: 1) PYE medium, a peptone and yeast extract based medium described in Walker et al, (1994) [supra], and 2) M6HiGG medium, a defined medium described in: Smit, J., et al 1981. “Caulobacter crescentus Pilin: Purification, Chemical Characterization and Amino-Terminal Amino Acid Sequence of a Structural Protein Regulated During Development”. J. Biol. Chem. 256, 3092-3097. The latter medium is especially appropriate for preparation of the aggregated chimeric proteins since it permits growth to higher densities (therefore maximizing protein yield) and results in purer aggregated proteins since there are no medium derived proteins to contaminate the chimeric proteins retrieved.

[0113] B—Creating Fusions of desired sequences with C-terminal portions of rsaA—Method 2.

[0114] Methods other than the use of the Carrier cassette plasmids are possible to create heterologous insertions into the deletion versions of rsaA or to create fusions with C-terminal portions of rsaA. PCR may be used although other known methods may also be used. The general procedure is as follows:

[0115] 1) Use PCR to prepare appropriate segments

[0116] a) Preparation of amplified segment with appropriate ends is carried out in a manner similar to that described part A(1)(a) above. Oligonucleotides are designed and synthesized such that they will anneal to appropriate regions of the desired heterologous DNA and also contain “sticky ends” of appropriate sequence and frame so that the resulting PCR product can be directed inserted into appropriate modified rsaA genes.

[0117] b) Transfer to appropriate C-terminal rsaA segments is carried out by inserting the PCR products into the C-terminal segments AA782-1026, AA905-1026, or AA944-1026, as described in Examples 7d-7g above. In addition to the BamHI site described, the EcoR1 restriction site could also be used as the 5′ terminus of the incoming PCR segment, since this site is also available in the pUC8 vector and not in the rsaA gene, so long as the correct reading frame was maintained when designing the oligonucleotides used to prepare the PCR product.

[0118] 2) Expression of the desired fusion in an appropriate C. crescentus host strain is carried out using the procedures outlined in part A(3) above.

[0119] C—Creating insertions of desired sequences into versions of the rsaA which have large internal in-frame deletions.

[0120] The general process is as follows:

[0121] 1) Creating appropriate in-frame deletions.

[0122]rsaA (ΔAA95-782) and rsaA(ΔAA188-782) were prepared as described above. Because most of the BamH1 linker insertion sites are in the same reading frame with respect to each other, it is possible to combine other pairs of 5′ and 3′ segments using the same general method, with the same result of maintenance of correct reading frame throughout. These deletion versions of rsaA must then be tested individually to ensure that they are still secreted by Caulobacter.

[0123] 2) Insertion of a Gene Segment Carrier cassette containing the desired sequences, prepared as described at part A(1) above, is carried out using the procedure described in part A(2) above.

[0124] Example 7h. Insertion of the 109 AA IHNV segment into rsaA (ΔAA95-782) and insertion of the 109 AA IHNV segment into rsaA(ΔAA188-782) is carried out as in Examples 7d-7g above. Expression of the desired genetic construction in appropriate C. crescentus strains is done using the procedures outlined in part A(3) above.

[0125] 3) Alternately, PCR procedures can be used to prepare a heterologous segment for direct insertion into the BamHI site with the deletion versions of the rsaA gene. The procedure is essentially the same as described in part B(1) above.

[0126] Example 8. Transfer to the native S-layer gene chromosomal site as a single crossover event.

[0127] The fusion of the Carrier cassette with appropriate heterologous DNA segments to a C-terminal rsaA segment plasmid results in a pUC8-based plasmid that is not maintained in Caulobacter. Selection for the antibiotic marker on the plasmid results in detection of the rescue events. Most commonly these are single crossover homologous recombination events. The result is a direct insertion of the entire plasmid into the chromosome. Thus the resident copy of rsaA remains unchanged as well as the incoming highly modified rsaA gene. In such cases it may be desirable to use Caulobacter strains in which the resident rsaA gene is inactivated in known ways. One example is the use of C. crescentus strain CB15AKSac; this strain has an antibiotic resistance gene cassette introduced at a position in the rsaA gene about 25% of the way from the 5′ terminus.

[0128] Example 9. Transfer to the native S-layer gene chromosomal site as a double crossover event.

[0129] In certain cases it may be desirable to completely exchange the resident rsaA gene copy with the incoming highly modified version. One method is the incorporation of a sacB gene cassette (Hynes, M. F., et al. 1989. “Direct Selection for Curing and Deletion of Rhizobium Plasmids Using Transposons Carrying the Bacillus subtilis sacB Gene.” Gene 78: 111-119) into the pUC8 based plasmids carrying the desired rsaA-heterologous gene construction. This cassette contains a levansucrase gene from Bacillus subtilis that, in the presence of sucrose, is thought to result in the production of a sugar polymer that is toxic to most bacteria when expressed inside the cell. One first selects for the single crossover event as described in Example 8. Subsequent growth on sucrose-containing medium results in the death of all cells except those that lose the offending sacB gene by homologous recombination within the 2 adjacent gene copies. Two events are possible; restoration of the resident copy of the rsaA or replacement of the resident copy with the incoming modified gene (the latter is the desired event). A screen with insertion DNA as probe or antibody specific to the heterologous gene product identifies successful gene replacement events. The method requires that rsaA gene sequence or native sequence immediately adjacent to the rsaA gene be on both sides of the heterologous sequence (ie, Carrier cassette sequence plus heterologous DNA) and in the present case is best suited for the deletion versions of the rsaA gene.

[0130] Other methods are available for the delivery of genes to the chromosome of C. crescentus. Methods involving the use of the transposons Tn5 and Tn7 as a means of delivery of genes to random chromosome locations are available (see: Barry, G. F. 1988 “A Broad-Host-Range Shuttle System for Gene Insertion into the Chromosomes of Gram-Negative Bacteria.” Gene 71:75-84.). The use of the xylose utilization operon as a target for chromosome insertion have also been described. This method involves the incorporation of a portion that operon into the pUC8 based plasmid constructions described above. This allows homologous recombination within the xylose operon as a means of plasmid rescue. Loss of the the ability to use xylose as a nutrition source is used as the means of confirming the rescue event.

[0131] This invention now being described, it will be apparent to one of ordinary skill in the art that changes and modifications can be made thereto without departing from the spirit or scope of the appended claims. 

We claim:
 1. A DNA construct comprising in sequence, one or more restriction sites for facilitating insertion of DNA to the construct and, DNA encoding at least the C-terminal region of the rsaA protein of C. crescentus, wherein the C-terminal region comprises at least amino acids 944-1026 of the rsaA protein. 